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SNP ID:
rs6690215
Gene
CR2
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.1: 207482705 - 207482705 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

TTGGTGAGGATGCAAAGCAAATGGT[C/T]AATATTTGGGAGTTTTAATCAGGAA

Assay ID C__30168452_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 63 submissions

Phenotype:

 MIM: 120650

Literature Links:

 CR2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.47)
(0.53)
Caucasian - Not Available CEPH (CEU)
C (0.42)
(0.58)
EAS
T (0.48)
(0.52)
African American - Not Available YRI (Yoruba)
T (0.40)
(0.60)
SAS
C (0.43)
(0.57)
Chinese - Not Available JPT (Japanese)
T (0.49)
(0.51)
AFR
T (0.41)
(0.59)
Japanese - Not Available CHB (Han Chinese)
T (0.34)
(0.66)
EUR
C (0.42)
(0.58)
AMR
C (0.30)
(0.70)
CR2 - complement component 3d receptor 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001006658.2 Intron NP_001006659.1
NM_001877.4 Intron NP_001868.2
XM_011509206.2 Intron XP_011507508.1

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